RS58730926 KRT17

Health Risk Chr 17:41624230
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What This Variant Does
"[OMIM:?]
Associated Conditions
Steatocystoma multiplex
Pachyonychia congenita 2
Inborn genetic diseases
Steatocystoma multiplex
Pachyonychia congenita 2
Inborn genetic diseases
Other Variants in KRT17
rs28928896 rs59151893 rs28933088 rs28928897 rs28928898 rs57674130 rs28928899 rs28933089 rs59977263 rs56690581
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